Tunca, Ekrem; Bulbul, Metin; Ilkimen, Halil; Canlidinc, Rukiye Saygili; Yenikaya, Cengiz published the artcile< Investigation of the effects of the proton transfer salts of 2-aminopyridine derivatives with 5-sulfosalicylic acid and their Cu(II) complexes on cancer-related carbonic anhydrases: CA IX and CA XII>, Reference of 21901-29-1, the main research area is cancer sulfosalicylic acid aminopyridine carbonic anhydrase IX XII.
Abstract: Six novel proton transfer compounds (15-20) obtained from 5-sulfosalicylic acid (1) and 2-aminopyridine derivatives [2-amino-3-benzyloxypyridine (2), 2-amino-3-hydroxylpyridine (3), 2-amino-3-methylpyridine (4), 2-amino-3-nitropyridine (5), 2-amino-3-nitro-4-methylpyridine (6) and 2-amino-3-nitro-6-methylpyridine (7)] and their Cu(II) complexes (21-26) along with the Cu(II) complexes of 2-7 (9-14) have been prepared and characterized by spectroscopic techniques. The in vitro inhibition effects of all compounds on CA IX and CA XII isoenzymes as well as on hCA I and hCA II were investigated and the results were compared. The inhibition studies showed that the synthesized compounds are more selective to CA XII isoenzyme. The hydratase IC50 values of the compounds were determined as in the range of 15.61 ± 2.32 uM-99.02 ± 4.99 uM for hCA I, 22.36 ± 0.75 uM-77.03 ± 4.03 uM for hCA II, 23.90 ± 1.67 uM-138.63 ± 5.45 uM for CA IX, and 9.50 ± 1.16 uM-693.15 ± 8.96 uM for CA XII. The inhibition data have been analyzed using one-way anal. of variance for multiple comparisons (p < 0.0001). Chemical Papers published new progress about Enzyme inhibition kinetics. 21901-29-1 belongs to class pyridine-derivatives, and the molecular formula is C6H7N3O2, Reference of 21901-29-1.